An efficient and stereoselective construction of the C(9)–C(17) dihydropyran segment of swinholides A–C via a novel reductive cleavage of an epoxy aldehyde
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Add time:08/28/2019 Source:sciencedirect.com
An efficient and highly stereoselective construction of the C(9)–C(17) dihydropyran segment of swinholides A–C, which involves a novel reductive cleavage of an epoxy aldehyde by an organoselenium reagent and the intramolecular conjugate addition of an acetal alkoxide anion of δ-hydroxy-α,β-unsaturated ester as the key steps, is described.
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